End-User Email Address required from July 1, 2020
In order to comply with the European Medical Device Regulation (MDR), manufacturers need to make sure that end users can be informed immediately about any recalls or safety-related issues concerning the products they are using.
For this reason, we will ask you to provide a valid email address for your end user, whenever you order license activations or trial extensions. Please note that - starting from July 1, 2020 - we will not activate any licenses without such an end-user email address. Of course, this data will be exclusively used for product recalls or safety-related information and not for marketing purposes.
Thank you for your understanding.